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Prevention of chemotherapy-induced nausea and vomiting: focus on fosaprepitant

机译:预防由化学疗法引起的恶心和呕吐:关注福沙普瑞特

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摘要

Fosaprepitant is a prodrug of aprepitant, a neurokinin1 (NK1) receptor antagonist used in prophylactic antiemetic regimens used prior to cytotoxic chemotherapy. Fosaprepitant is being developed to provide a parenterally administered alternative to the orally administered aprepitant. Fosaprepitant is rapidly converted to aprepitant and an intravenous dose of 115 mg is bioequivalent to 125 mg orally, with similar plasma concentrations at 24 hours. In phase I and II trials fosaprepitant shows efficacy, but the large randomized efficacy studies have utilized aprepitant. When it is added to dexamethasone and a 5HT3 receptor antagonist on day 1 prior to chemotherapy aprepitant improves the control of acute post chemotherapy emesis and when continued on days 2 and 3 with dexamethasone it demonstrated even greater improvement in the control of delayed emesis. This has been shown with both cisplatin-containing regimens and those based upon cyclophosphamide and an anthracycline. Fosaprepitant is well tolerated with mild to moderate venous irritation being the only additional toxicity to those seen with oral aprepitant, and that is a function of dose, concentration, and infusion rate. Headaches are the other toxicity most commonly reported. Fosaprepitant can be used as a parenteral alternative to aprepitant in regimens to control chemotherapy-induced emesis.
机译:Fosaprepitant是aprepitant的前药,aprepitant是一种神经激肽(NK1)受体拮抗剂,用于细胞毒性化学疗法之前的预防性止吐方案。正在开发Fosaprepitant,以提供口服给药的非处方药的肠胃外替代药物。 Fosaprepitant迅速转变为aprepitant,静脉注射115 mg相当于口服125 mg具有生物等效性,并且24小时血浆浓度相似。在第一和第二阶段的试验中,福沙雷匹坦显示疗效,但大量的随机疗效研究已使用了阿雷匹坦。当在化疗前第1天将地塞米松和5HT3受体拮抗剂添加到地塞米松和5HT3受体拮抗剂中时,prepitant改善了对急性呕吐的控制,而在地塞米松的第2天和第3天继续使用时,证明在延迟呕吐的控制上甚至有更大的改善。这在含顺铂的方案和基于环磷酰胺和蒽环类的方案中均已显示。 Fosaprepitant具有良好的耐受性,轻度至中度的静脉刺激是口服aprepitant所见毒性的唯一附加毒性,并且是剂量,浓度和输注速率的函数。头痛是最常见的其他毒性反应。在控制化疗诱导的呕吐的治疗方案中,福沙普瑞汀可以用作阿普瑞汀的肠胃外替代药物。

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